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Infection and Drug Resistance logoLink to Infection and Drug Resistance
. 2021 Dec 7;14:5209–5217. doi: 10.2147/IDR.S333421

Analysis of Bacterial Biofilm Formation in Patients with Malignancy Undergoing Double J Stent Indwelling and Its Influencing Factors

Ke Zeng 1,*, Jia-Mo Zhang 2,*, Xiao-Bin Li 1, Sheng-Xian Peng 3, Su-Chuan Zhang 4, Wen-Xian Xie 5, Chun-Fang Xi 1, Cheng-Jian Cao 6,
PMCID: PMC8666721  PMID: 34916809

Abstract

Objective

To analyze the bacterial biofilm (BF) formation in patients with malignancy undergoing double J stent indwelling and its influencing factors.

Methods

A total of 167 patients with malignant tumors who received double J stent indwelling in the hospital from January 2018 to January 2021 were included in the study. The urine and double J stent samples were collected for bacterial identification and observed for BF formation on the surface of the urinary catheter under a scanning electron microscope (SEM). Univariate and multivariate logistic regression analyses were used to analyze the influencing factors of BF.

Results

The BF formation rate was 34.73% (58/167). The BF formation rate of positive specimens cultured in urine and double J stent was significantly higher than that of negative ones (P<0.05). Staphylococcus was the main BF bacteria in double J stent and urine culture specimens, followed by Enterococcus, Pseudomonas, Enterobacter, and Acinetobacter. Compared with the non-BF group, the number of viable bacteria in the double J stent and urine and the catheterization time in the BF group rose markedly (P<0.05). Advanced age, chemotherapy, anemia, indwelling time ≥90d, and urinary tract infection were risk factors for BF formation in patients with malignancy undergoing double J stent indwelling (P<0.05).

Conclusion

There is a high rate of BF formation in patients with malignancy undergoing double J stent indwelling, with Staphylococcus as the dominant species. Treatment requires enhanced urinary catheter management and nutritional status to inhibit BF formation and lower the rate of urinary catheter-related infections.

Keywords: malignant tumor, double J stent indwelling, biofilm, catheter-related infection, etiology, influence factor

Introduction

Double J ureteral stent, frequently used for indwelling ureter, can effectively relieve ureteral obstruction and prevent ureteral stenosis.1 Consequently, preoperative or intraoperative indwelling double J stent is a common measure to prevent ureteral injury2 as well as postoperative upper urinary tract obstruction due to surgery or metastasis of tumor in patients with malignant tumors, especially gynecological and urinary malignant tumors.3 However, its therapeutic effect is undermined by complications, such as urinary tract infection and urinary sepsis in severe cases, which threatens the life and health of patients.4 It has been confirmed by relevant research that bacteria biofilm (BF) formation, membrane-like substances formed by bacteria adhering to the surface, can enable bacteria to develop drug resistance against antimicrobial agents.5 As a result, it is considered that the formation of BF may be a key contributory factor to the relapse and intractability of urinary tract infections.6 Therefore, the analysis of BF formation in patients with malignancy undergoing double J stent indwelling and the exploration of factors affecting urinary tract infection in patients are of great significance for clinical treatment. The results are reported as follows.

Data and Methods

Clinical Data

A total of 167 patients with malignant tumors who received double J stent indwelling in the hospital from January 2018 to January 2021 were included in the study. Inclusion criteria: ① 18–80 years old; ② malignant tumors confirmed by pathology; ③ the double J stent was indwelling for the first time, with the indwelling time no less than 30 d; ④ COOK(UFH-626, USI-626-CE-B) double J stent was used; ⑤Estimated survival time ≥6 months. Exclusion criteria: ①urinary tract infection existed before the double J stent indwelling; ②double J stent indwelling contradiction; ③ failure in double J stent indwelling; ④Infection occurred due to other reasons after operation; ⑤ urological tumors such as epithelial tumors of the upper urinary tract. The study was approved by the Hospital Ethics Committee of First people’s hospital of Zigong city and the patients signed an informed consent form. The study was in accordance with the Helsinki Declaration as revised in 2013 for experiments involving humans.

Methods

General Information Collection

General information, including the patients’ age, gender, height, weight, highest educational level, hypertension, diabetes mellitus, hormone therapy, chemotherapy, radiotherapy, tumor clinical stage, tumor type, anemia, double J stent indwelling time, the presence of urinary tract infection, and the type of urinary tract infection was recorded. Body Mass Index (BMI)= Weight (kg) divided by the square of Height (m).

Specimen Collection

After routine disinfection, draping, and local anesthesia, 3 mL of urine was collected by a disposable sterile syringe by urethral catheterization, and the double J stent was removed under a cystoscopy or ureteroscopy. The bladder pelvis segment was divided into two segments for observation, each about 3 cm long. One segment was observed under Scanning Electron Microscope (SEM) on the BF morphology on the surface of the double J stent. The other section of the double J tube was placed in the inoculation bottle, added with 30 mL of physiological saline, and eluted by the vortex shaker at 3000 R/min for 1 minute. Subsequently, the precipitate was inoculated into blood agar plate medium and MacConkey agar medium, and placed in a constant temperature incubator at 37°C for 16 to 24 hours. The formation of sterile colonies was observed, and the bacterial species and drug sensitivity were identified.

Observation on BF Morphology on Double J Stent Surface and Counting of Viable Bacteria Colony

In the groups of 30–60 days, 61–90 days, 91–120 days, 121–150 days, and more than 150 days, 5 specimens of double J stent were selected from each group by random number table method. The double J stent was rinsed with PBS solution three times, 10 min each. The samples were fixed with osmic acid for 1 h and rinsed with PBS solution three times, 10 min each. The dehydration was carried out in gradient with 30%, 50%, 70%, 80%, 90%, and 100% trimethyl methanol, respectively, and repeated for three times. After drying with a high-vacuum coating apparatus for 20–30 min, the specimens of double J stent were scanned by a SEM (S3000N, Hitachi, Japan) after gold spraying, and six fields of 100 μm were randomly selected for each specimen. The formation of BF on the surface of the double J stent was observed and photographed, and the viable bacterial colonies were counted. It is defined as BF if meeting the following morphological characteristics: water channel, three-dimensional structure, spherical or elliptical corpuscle coated with matrix.

Viable Bacteria Counting and Bacterial Identification

1 mL each of clean urine and double J stent rinsing fluid were collected, and viable bacteria counts were analyzed with a UF-1000i automatic urine analyzer from SYSMEX. Urine specimens and double J stent specimens were inoculated on blood agar plates (Zhengzhou Antu Company). All the specimens were identified in accordance with the national clinical inspection operating procedures. Vitek 2 compact automatic bacteria identification drug susceptibility instrument (Mérieux Company, France) was used to identify the bacteria, and the reagents were the matching GN, GP identification cards and GN13, GP67 drug susceptibility cards.7

Diagnosis Criteria8

The occurrence of urinary infection within 48 h after indwelling or removal of double J stent was considered as urinary infection associated with double J stent. Urinary infection was diagnosed with urine bacterial culture containing Gram-positive cocci ≥104CFU/mL and Gram-negative bacilli ≥105CFU/mL.

Statistical Methods

SPSS20.0 software was used for statistical analysis. Measurement data conforming to normal distribution were expressed as (Inline graphic±s). Independent sample t-test was used for comparison between groups, paired sample t-test for intra-group comparison, one-way analysis of variance for comparison among groups, and Sink-q test for pairwise comparison. The enumeration data were expressed by frequency or ratio and analyzed using the Karman non-correction method, with the total cases no less than 40 and the minimum theoretical frequency over 5. Logistic regression was used to analyze the risk factors. P < 0.05 indicated that the difference was statistically significant.

Results

General Information About Double J Stent Indwelling Patients with Malignant Tumors

Patients’ general information is presented in Table 1.

Table 1.

General Data of Malignant Tumor Patients with Indwelling Double J Stent (n=167)

Item Number of Cases Ratio (%)
Age
 < 60 years old 78 46.71
 ≥60 years old 89 53.29
Gender
 Male 71 42.51
 Female 96 57.49
BMI
 18.5~22.9kgm2 57 34.13
 23.0~27.4kgm2 86 51.50
 ≥27.5kgm2 24 14.37
Highest level of education
 Junior secondary and below 44 26.35
 Senior high school and
 technical Secondary school
69 41.32
 College and above 54 32.34
High blood pressure
 Yes 96 57.49
 No 71 42.51
Diabetes
 Yes 65 38.90
 No 102 61.10
Hormone therapy
 Yes 43 25.75
 No 124 74.25
Chemotherapy
 Yes 113 67.66
 No 54 32.34
Treat by radiation therapy
 Yes 56 33.53
 No 111 66.47
Clinical stages
 I–II 79 47.31
 III–IV 88 52.69
Malignant tumor type
 Digestive system 44 26.35
 Urinary system 62 37.13
 Gynecology 38 22.75
 Others 23 13.77
Anaemia
 Yes 63 37.72
 No 104 62.28
Stenting duration
 30~60d 21 12.57
 61~90d 48 28.74
 91~120d 56 33.53
 121~150d 28 16.77
 ≥151d 14 8.38

Formation of BF of Urine and Double J Stent Specimens

The BF formation rate in 167 malignant tumor patients with double J stent indwelling was 34.73% (58/167). Positive specimens cultured in urine and double J stent showed a remarkably higher formation rate of BF than those negative specimens (P < 0.05). See Table 2.

Table 2.

Formation of Urinary Stent BF in Double J Stent Indwelling Patients with Malignant Tumors

Item Result Number of Cases BF Formation χ2 P
Number of Cases Formation Rate (%)
Urine culture Positive 45 11 24.4 12.01 <0.001
Negative 122 5 4.09
Double J stent culture Positive 78 58 74.36 13.22 <0.001
Negative 89 3 3.37

The Changes of Double J Tube Electron Microscope Monitoring of Patients in Each Group

BF formation is observed on various surfaces. After 30 days, the bacteria on the surface of the double J stent were few and scattered, and covered by a large number of fibrous membranes. Inconsistent amounts of inflammatory attachments and crystals were observed on the surface of the double J stent (Figure 1A). At 90 days, piles of colonies on the surface of the double J stent were observed, and most were cocci (Figure 1B). The number of bacterial colonies in the ducts was (1.73±0.59), (2.26±1. 19), (4. 68±1.31), (5.71±1.06), (7.76±1.37) CFU/cm2 in each group, respectively (P<0.05). It shows that bacterial colonies, inflammatory attachments, crystals, and bacterial biofilm on the surface of the double J stent increase with the extend of the double J tube indwelling time.

Figure 1.

Figure 1

BF morphology on the surface of double J (SEM, ×600).

Notes: (A) no BF formation. SEM shows normal grooves and depressions, no adhesions on the surface; (B) BF formation. SEM shows the presence of polymorphism in the inner wall of the ureter, partly with single or multiple bacterial adhesions, and visible stereospecific structure formation.

Bacterial Identification of BF in Double J Stent of Patients

A total of 58 strains of biofilm-positive bacteria were screened out from 78 positive specimens cultured in a double J stent. The results showed that Staphylococcus was the main type of bacteria in double J stent, followed by Enterococcus, Pseudomonas, Enterobacter, and Acinetobacter. See Table 3.

Table 3.

Bacterial Identification of BF in Double J Stent of Patients

Strain Bacterial Name Number of Plants Ratio (%)
Enterobacter hormaeche and edwards Escherichia coli 6 10.34
Enterococcus Enterococcus faecalis 14 24.14
Uroenterococcus 5 8.62
Pseudomonas Pseudomonas aeruginosa 5 8.62
Staphylococcus Staphylococcus epidermidis 11 18.97
Staphylococcus haemolyticus 7 12.07
Staphylococcus aureus 6 10.34
Acinetobacter Acinetobacter baumannii 4 6.90
Total 58 100.00

Bacterial Identification of BF in the Urine of Patients

Eleven strains of biofilm-positive bacteria were screened out from 45 positive urine-cultured specimens. After identifying the bacterial genus, it was found that the biofilm bacteria in the urine were mainly Staphylococcus, followed by Enterococcus, Pseudomonas, and Enterobacter, Acinetobacter, see Table 4.

Table 4.

Bacterial Identification of Urine BF in Patients

Strain Bacterial Name Number of Plants Ratio
Enterobacter hormaeche and edwards Escherichia coli 6 15.38
Enterococcus Enterococcus faecalis 16 41.03
Uroenterococcus 1 2.56
Pseudomonas Pseudomonas aeruginosa 1 2.56
Staphylococcus Staphylococcus epidermidis 6 15.38
Staphylococcus haemolyticus 4 10.26
Staphylococcus aureus 3 7.69
Acinetobacter Acinetobacter baumannii 2 5.13
Total 39 100.00

Comparison of Viable Counts of Bacteria - In Double J Stent and Urine of Patients in the BF-Forming Group and Non-BF-Forming Group

The viable count of bacteria in the double J stent and urine of patients of the BF-forming group exceeded that of the non-BF-forming group (P < 0.05). See Table 5.

Table 5.

Comparison of Viable Counts of BF in Double J Stent and in Urine of Patients Between the BF Forming Group and the Non BF Forming Group (Cells/μL, Inline graphic s)

Group Number of Cases Double J Stent Urine
BF forming group 58 1042.54±253.46 836.48±214.32
Non BF forming group 109 234.28±248.14 112.36±123.61
t 19.893 27.701
P <0.001 <0.001

Comparison of Double J Stent Indwelling Time Between Groups with and without BF Formation

A markedly longer double J stent indwelling time was recorded with patients in the BF-forming group in comparison with the non-BF-forming group (P < 0.05). See Table 6.

Table 6.

Comparison of Double J Stent Time of Patients in the BF Forming Group and Non BF Forming Group (d, Inline graphic s)

Group Number of Cases Stent Setting Time
BF forming group 58 18.93±2.48
Non BF forming group 109 8.14±2.31
t 28.011
P <0.001

Comparison of Viable Counts Of Bacteria in Double J Stent and Urine of Patients with Different Double J Stent Indwelling Time

As the stenting duration increased, the viable count of bacteria in the double J stent and urine grew significantly (P < 0.05). See Table 7.

Table 7.

Comparison of Viable Counts of Biofilm in Double J Stent and Urine of Patients with Different Double J Stent Duration (Cells/μL, Inline graphic s)

Tube Setting Time Number of Cases Double J Stent Urine
30~60d 21 349.61±187.43 138.49±84.36
61~90d 48 512.43±195.82 298.69±80.41
91~120d 56 739.48±198.84 412.43±78.95
121~150d 28 993.16±201.15 647.15±81.47
≥151d 14 1134.14±214.36 834.18±85.64
F 59.767 236.852
P <0.001 <0.001

Analysis of the Influencing Factors BF Formation in Malignant Tumor Patients with Double J Stent Indwelling

Patients with an age of ≥60 years, female, diabetes, hormonal therapy, chemotherapy, anemia, long duration of tube indwelling, and urinary tract infection had significantly increased rates of ureteral BF formation (P < 0.05). See Table 8.

Table 8.

Analysis of Urinary Catheter BF Formation in Malignant Tumor Patients with Double J Stent Indwelling

Item Number of Cases BF Forming Group (n=58) Non BF Forming Group (n=109) 2 P
Age 18.184 <0.001
 < 60 years old 78 14 64
 ≥60 years old 89 44 45
Gender 6.340 0.012
 Male 71 17 54
 Female 96 41 55
BMI 5.154 0.076
 18.5~22.9kgm2 57 16 41
 23.0~27.4kgm2 86 29 57
 ≥27.5kgm2 24 13 11
Highest level of education 0.372 0.830
 Junior secondary and below 44 16 28
 Senior high school and
 technical secondary school
69 25 44
 College and above 54 17 37
High blood pressure 0.297 0.586
 Yes 96 35 61
 No 71 23 48
Diabetes 21.120 <0.001
 Yes 65 38 27
 No 102 21 81
Hormone therapy 40.240 <0.001
 Yes 43 32 11
 No 124 26 98
Chemotherapy 11.488 0.001
 Yes 113 49 64
 No 54 9 45
Treat by radiation therapy 0.036 0.850
 Yes 56 20 36
 No 111 38 73
Clinical stages 0.629 0.428
 I–II 79 25 54
 III–IV 88 33 55
Malignant tumor type 1.207 0.751
 Digestive system 44 16 28
 Urinary system 62 21 41
 Gynecology 38 15 23
 Others 23 6 17
Anemia 65.413 <0.001
 Yes 63 46 17
 No 104 12 92
Stent setting time 51.817 <0.001
 30~60d 21 4 17
 61~90d 48 5 43
 91~120d 56 16 40
 121~150d 28 21 7
 ≥151d 14 12 2
Urinary tract infection 38.498 <0.001
 Yes 45 11 34
 No 122 5 117
Type of urinary tract infection 22.474 0.215
 Symptomatic 21 14 7
 Asymptomatic 24 13 11

Logistic Regression Analysis for Multiple Factors of Urinary Catheter BF Formation in Malignant Tumor Patients with Double J Stent Indwelling

Advanced age, chemotherapy, anemia, indwelling time ≥90 d, and urinary tract infection were risk factors for BF formation in patients with malignancy undergoing double J stent indwelling (P < 0.05). See Table 9.

Table 9.

Multi-Factor Logistic Regression Analysis of Urinary Catheter BF Formation in Malignant Tumor Patients with Double J Stent Indwelling

Factor β SE Wald P OR (95% CI)
Age ≥60 years old 1.123 0.487 5.364 0.012 3.236 (1.198~7.456)
Chemotherapy 1.012 0.326 4.264 <0.001 3.697 (2.342~6.397)
Anaemia 1.214 0.418 6.978 <0.001 3.523 (2.971~7.448)
Catheter time 90 d or higher 1.435 0.523 11.751 <0.001 5.044 (1.893~11.784)
Urinary tract infection 1.237 0.272 8.233 <0.001 3.912 (1.292~8.396)

Discussion

Indwelling double J stent is a significant step to prevent upper urinary tract obstruction after malignant tumor surgery to achieve better quality of life.9 Relevant evidence suggests that the rate of catheter-associated urinary tract infections remains at a high level in recent years, which requires sufficient attention.10 The application of double J stent mainly plays a role in fixedly supporting the ureter, relieving the obstruction caused by ureteral edema and inflammation, and preventing postoperative anastomotic leakage and ureteral stenosis,11 which ensures a shorter bed rest and a better rehabilitation effect with no limitation and discomfort from the external drainage stent.12 However, it has been found that the presence of double J stent predisposes to urinary reflux in the ureter, resulting in a rise in the retrograde infection rate of the kidney.13 Zhou Honghui et al14 reported that the rate of urinary tract infection in patients with double J stent indwelling for early radical cervical cancer was about 22.95%. The rate of BF formation in this study (34.73%) was slightly higher than that reported by others14 and was related to the inclusion of gastrointestinal and urinary malignancies in this study. The high molecular materials such as polyurethane used in the double J stent facilitate the adherence of bacteria to its surface and the subsequent formation of BF. Prior research demonstrated that the formation of bacterial BF can increase its resistance by more than 1000 times15 and inhibit its antigenic expression to generate immune escape.16 In addition, under appropriate conditions, the bacteria in BF can diffuse and free from the membrane, causing re-infection.17

In this study, urine and double J stent specimens were collected from patients, respectively, and SEM observation revealed that BF formation was found in 39 of 45 positive urine culture specimens, which was consistent with the results of previous studies, and BF formation was found in 13 other negative urine culture specimens, which may be related to the fact that urine bacteria are mostly planktonic, thereby leading to false-negative results; however, the influence of native bacteria on the results was not excluded, which requires further analysis.18 Moreover, BF formation was found in 58 of 78 positive double J stent culture specimens, and no BF formation was found in negative double J stent culture specimens. These results suggest that the rate of BF formation is higher in patients with malignancy undergoing double J stent indwelling, and double J stent culture more accurately responds to bacterial colonization and BF formation in the urinary catheter than urine culture. The results of bacterial identification showed that Staphylococcus was the dominant type of bacteria in the double J stent and urine culture samples, followed by Enterococcus, Pseudomonas, Enterobacter, and Acinetobacter, which was basically in line with the previous research results.8,14 This suggested that, compared with other types of bacteria, Staphylococcus might be more prone to produce biofilm bacteria, which provides a reference for the selection of clinical antibacterial drugs.

Moreover, this study found that the viable count of bacteria in both double J stent and urine rose sharply with the increase of stenting duration, indicating that the risk of BF formation grew with the increase of stenting duration, which was confirmed by the results of electron microscope scan. In clinical practice, the application of indwelling double J stent requires strict management to reduce unnecessary use. To reduce the formation of BF, Double J stent requires regular replacement or the periodical evaluation of double J stent removal in a timely manner. Analysis of factors influencing the formation of BF in the urinary catheter in patients with malignancy undergoing double J stent indwelling found that patients with an age of ≥60 years, female, diabetes, hormonal therapy, chemotherapy, anemia, long duration of tube indwelling, and urinary tract infection had significantly increased rates of ureteral BF formation, and advanced age, chemotherapy, anemia, indwelling time ≥90 d, and urinary tract infection were risk factors for BF formation in patients with malignancy undergoing double J stent indwelling. It indicated that enhanced nutritional management for elderly patients, urethral care for female patients, and strict control of blood glucose levels in diabetic patients are warranted to reduce the rate of urinary catheter-related infections.

In conclusion, there is a high rate of BF formation in patients with malignancy undergoing double J stent indwelling, with Staphylococcus as the dominant species. Treatment requires enhanced urinary catheter management and nutritional status to inhibit BF formation and lower the rate of urinary catheter-related infections. The shortcoming of this study lies in the absence of characterization analysis of the isolates,19 which limits the determination of treatment protocols and will be explored in further studies.

Disclosure

The authors report no conflicts of interest in this work.

References

  • 1.Sundaramurthy S, Thomas RJ, Herle K, et al. Double J stent removal in paediatric patients by Vellore Catheter Snare technique: a randomised control trial. J Pediatr Urol. 2019;15(6):661–668. doi: 10.1016/j.jpurol.2019.08.009 [DOI] [PubMed] [Google Scholar]
  • 2.Haitao Y, Wei Z, Chunhong N. Comparison and analysis of ureteral stricture caused by malignant tumor treated by conventional surgery and minimally invasive double J stent retrograde insertion. Chin Basic Med. 2021;28(2):203–207. [Google Scholar]
  • 3.He JW, Shu G, Songtao X, et al. Analysis of clinical data of 96 cases of ureteral obstruction caused by gynecological malignant tumor. Chin J Endoscopy. 2020;26(2):65–69. [Google Scholar]
  • 4.Dengjun H, Yong L, Chan A, et al. Effect of pre-set double J stents on complications of flexible ureteroscopic lithotripsy in kidney calculi. Med J Qilu. 2017;155(5):87–89. [Google Scholar]
  • 5.Rajput A, Thakur A, Sharma S, et al. aBiofilm: a resource of anti-biofilm agents and their potential implications in targeting antibiotic drug resistance. Nucleic Acids Res. 2018;46(D1):894–900. doi: 10.1093/nar/gkx1157 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Betschart P, Zumstein V, Buhmann MT, et al. Symptoms associated with long-term double-J ureteral stenting and influence of biofilms. Urology. 2019;134(4):72–78. doi: 10.1016/j.urology.2019.08.028 [DOI] [PubMed] [Google Scholar]
  • 7.Hong S, Yushan W, Ziyu S. National operating procedures for clinical examination. People’s Health Publishing House; 2015. [Google Scholar]
  • 8.Yuncai Y, Junlin Z, Jianming C. Characteristics and drug resistance of pathogens causing catheter-related urinary tract infection. Chin J Disinfect. 2017;34(10):986–988. [Google Scholar]
  • 9.AI-ling Z, Qiong-feng X, Fang-lei X, et al. Analysis of influencing factors of time of indwelling catheter for patients with benign prostatic hyperplasia and malignant tumor after operation. Chin J Mod Nurs. 2017;23(13):1718–1723. [Google Scholar]
  • 10.Mingrong S, Wenzhi H, Quanhui W. Investigation on prevalence rate of catheter-related urinary tract infection from 2012 to 2018. Chin J Nosocomiol. 2020;30(15):91–95. [Google Scholar]
  • 11.Alnadhari I, Alwan MA, Salah MA, et al. Treatment of retained encrusted ureteral double-J stent. Arch Ital Urol Androl. 2019;90(4):265–269. doi: 10.4081/aiua.2018.4.265 [DOI] [PubMed] [Google Scholar]
  • 12.Wuxue LI, Zhao X, Changbao XU, et al. Clinical observation of time of double J stent indwelling in treatment of complex ureteral calculi with ureteroscope. J Pract Med. 2017;33(2):256–258. [Google Scholar]
  • 13.Shi ZJ, Qiong Z, Lixin J, et al. Analysis of clinical characteristics of double J stent urinary system infection. J Wuhan Univ. 2020;41(3):109–113. [Google Scholar]
  • 14.Zhou HH, Wang N, Ding JJ. Etiological characteristics and influencing factors of urinary tract infection in patients with double J stents indwelling in radical hysterectomy for early cervical cancer. Chin J Nosocomiol. 2019;29(18):2839–2842. [Google Scholar]
  • 15.Goswami S, Sarkar R, Saha P, et al. Effect of human placental extract in the management of biofilm mediated drug resistance - A focus on wound management. Microb Pathog. 2017;111(34):307–315. doi: 10.1016/j.micpath.2017.08.041 [DOI] [PubMed] [Google Scholar]
  • 16.Jia L, Sun L, Wei L, et al. A nuclease from Streptococcus mutans facilitates biofilm dispersal and escape from killing by neutrophil extracellular traps. Front Cell Infect Microbiol. 2017;28(7):97–99. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Heim CE, Bosch ME, Yamada KJ, et al. Lactate production by Staphylococcus aureus biofilm inhibits HDAC11 to reprogramme the host immune response during persistent infection. Nat Microbiol. 2020;5(10):1271–1284. doi: 10.1038/s41564-020-0756-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Zhang JZ. Exploration on related factors and preventive measures of indwelling urethral catheterization in urinary system infection of hospital. Contemp Med. 2017;23(6):116–117. [Google Scholar]
  • 19.Gajdács M, Kárpáti K, Stájer A, et al. Insights on carbapenem-resistant Pseudomonas aeruginosa: phenotypic characterization of relevant isolates. Acta Biologica Szegediensis. 2021;65(1):105–112. doi: 10.14232/abs.2021.1.105-112 [DOI] [Google Scholar]

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